Schwartz Christopher J, Schandl Cynthia A, Morse Jennifer, Ralston Jonathan, Rapkiewicz Amy, Darvishian Farbod
1 New York University Medical Center, New York, NY, USA.
2 Medical University of South Carolina, Charleston, SC, USA.
Int J Surg Pathol. 2018 Sep;26(6):488-493. doi: 10.1177/1066896918763901. Epub 2018 Mar 19.
Myxoid lesions of the breast can be diagnostically challenging entities. We report 4 cases of CD34+ fibromyxoid lesion that have been previously diagnosed as "benign myxoid lesion," "nodular mucinosis," or "mammary myofibroblastoma, myxoid type" on the basis of CD34-positivity. The lesions were microscopically well circumscribed and composed of a paucicellular spindle cell proliferation in a background of myxoid stroma. No epithelial component was identified. The spindle cells showed immunohistochemical reactivity for CD34 and smooth muscle actin. Based on morphologic and immunohistochemical similarities between these cases and myxoid myofibroblastoma, we compared 4 myxoid lesions with cases of typical myofibroblastoma, utilizing retinoblastoma (Rb) antibody and fluorescent in situ hybridization for 13q14 gene rearrangement (encoding the Rb gene). The myxoid lesions showed retention of Rb protein by immunohistochemistry, whereas Rb expression was lost in cases of myofibroblastoma. We identified loss of 13q14 in 3 of 4 cases of myofibroblastoma. Notably, 13q14 gene rearrangement was not observed in any of the myxoid lesions. Our data show that there is at least a subset of CD34+ fibromyxoid lesions that, despite overlapping morphologic and immunohistochemical phenotype and proposed common histogenesis with myofibroblastomas, is genetically distinct from the latter based on Rb analysis.
乳腺黏液样病变在诊断上可能具有挑战性。我们报告4例CD34+纤维黏液样病变,这些病变先前基于CD34阳性被诊断为“良性黏液样病变”“结节性黏液变性”或“黏液样型乳腺肌纤维母细胞瘤”。病变在显微镜下边界清晰,由黏液样基质背景中细胞稀少的梭形细胞增生组成。未发现上皮成分。梭形细胞对CD34和平滑肌肌动蛋白呈免疫组化反应。基于这些病例与黏液样肌纤维母细胞瘤在形态学和免疫组化上的相似性,我们利用视网膜母细胞瘤(Rb)抗体和荧光原位杂交检测13q14基因重排(编码Rb基因),将4例黏液样病变与典型肌纤维母细胞瘤病例进行比较。黏液样病变通过免疫组化显示Rb蛋白保留,而肌纤维母细胞瘤病例中Rb表达缺失。我们在4例肌纤维母细胞瘤中的3例中发现13q14缺失。值得注意的是,在任何黏液样病变中均未观察到13q14基因重排。我们的数据表明,至少有一部分CD34+纤维黏液样病变,尽管在形态学和免疫组化表型上与肌纤维母细胞瘤重叠,且推测有共同的组织发生,但基于Rb分析,其在基因上与后者不同。